Author:
Ferreira Regina Moreira,Fernandes Pedro Luiz,Machado Avelino Luz
Abstract
Da análise retrospectiva de 21 casos de crianças tratadas de “Tumor de Wilms" entre 1982-1986, obtivemos taxa de sobrevida de 81% em 5 anos. Os pacientes que apresentaram evolução de doença a apresentaram em abdome. A abordagem terapêutica correta o mais precoce possível torna este tumor curável na maioria dos casos.
Publisher
Revista Brasileira De Cancerologia (RBC)
Reference10 articles.
1. Beckwith JD, Palmer NF. Flistopathology and prognosis ot Wilms Tumor: Resuits from the first National Wilms’ Tumor Study Câncer. Câncer 1978,41 (5): 1937-1948.
2. Breslow NE, Palmer NF, HilI LR, era/. Wilms Tumor: Prognostic factors for patients without metastases at diagnosis. Resuits of the National Wilms Tumor Study. Câncer 1978, 41 (4): 1577-1589.
3. D’Angio GJ, Evans AE, Breslow N, era/. Resuits of the third National Wilms' Tumor Study. Proceedings of the American Association for Câncer Research 1984,25: 183.
4. D’Angio GJ, Evans AE, Breslow N, etal. The treatment of Wilms’ Tumor: Results of the National Wilms’ Tumor Study. Câncer 1976, 38: 633-646.
5. Lemerle J, Voute PA, lournade MF, etal. Preoperative versus post operative radiotherapy, single versus multiple courses of Actinomycin-D In the treatment of Wilms’ Tumor. Câncer 1976, 38: 647-654.